A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551853



Internal ID20924986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26980095..26980588hg38UCSC Ensembl
chr1:27306586..27307079hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551853
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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